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Titlebook: Manual of Soft-Tissue Tumor Surgery; Walter Lawrence,James P. Neifeld,Jose J. Terz Book 1983 Springer-Verlag New York Inc. 1983 Rehabilita

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Book 1983ustrated herein. We are indebted to Dr. Saul Kay, Professor of Pathology, and Dr. James Walsh, Associate Professor of Radiology, for providing the illustrations of histopathology and radiologic imaging in the early chapters. We particularly appreciate the superb artwork of our enthusiastic teammates
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0172-4827 ent is illustrated herein. We are indebted to Dr. Saul Kay, Professor of Pathology, and Dr. James Walsh, Associate Professor of Radiology, for providing the illustrations of histopathology and radiologic imaging in the early chapters. We particularly appreciate the superb artwork of our enthusiastic teammates978-1-4612-5556-7Series ISSN 0172-4827
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Soft-Tissue Sarcomas: Etiology, Pathology, and Clinical Featuressarcomas diagnosed each year in the United States is about 5000. In view of this, few surgeons have had enough experience with these lesions to appreciate the many variations in their clinical presentation or natural history. Also, owing to this limited incidence of sarcomas, few controlled clinical
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Operative Treatment of Soft-Part Sarcomastment of choice for most primary tumors. Adjuvant therapy with radiation might well affect the scope of the operation employed, and the data available for defining the value of this adjuvant treatment will be discussed in Chapter 11. The major treatment decision for sarcomas relates to the extent of
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Operations for Sarcomas on the Lower Extremityas. Both the anatomy and bulk of tissue in this site often allow an adequate soft-part resection in terms of tumor margin, and “limb salvage” can be achieved. It is also possible in many instances to obtain an adequate local margin around the sarcoma by wide but intracompartmental excision. However,
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Retroperitoneal Sarcomasroperitoneal sarcomas in children are discussed in Chapter 13). When considering malignant tumors of the retroperitoneal space, other than those arising in the kidney or adrenal gland, the incidence of soft-tissue sarcomas ranges from 43% to 70%, with lymphomas comprising from 15% to 32% of the tota
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